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CODEX: a normalization and copy number variation detection method for whole exome sequencing

High-throughput sequencing of DNA coding regions has become a common way of assaying genomic variation in the study of human diseases. Copy number variation (CNV) is an important type of genomic variation, but detecting and characterizing CNV from exome sequencing is challenging due to the high leve...

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Vydáno v:Nucleic Acids Res
Hlavní autoři: Jiang, Yuchao, Oldridge, Derek A., Diskin, Sharon J., Zhang, Nancy R.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2015
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4381046/
https://ncbi.nlm.nih.gov/pubmed/25618849
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gku1363
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